Taiwan FDA registration b109208b69b9e28310c664ac6579faca
“Ivoclar Vivadent” Telio Inlay/Onlay
TW: “義獲嘉偉瓦登特”特利歐牙科嵌體材料
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Jul 24, 2021 – Jul 24, 2026ExpiredRegistration details
- Analysis ID
- b109208b69b9e28310c664ac6579faca
- License Form
- Ministry of Health Medical Device Import No. 034723
- Customs Code
- DHA05603472305
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3770 Temporary crown and bridge resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 24, 2021
- Expiry Date
- Jul 24, 2026
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Telio Inlay/Onlay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b109208b69b9e28310c664ac6579faca and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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